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Serveur d'exploration sur le lymphœdème - Curation (Istex)

Index « Auteurs » - entrée « Tsutomu Ogata »
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List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
002033 (2004) Rie Yoshida [Japon] ; Masafumi Miyata [Japon] ; Toshiro Nagai [Japon] ; Toshio Yamazaki [Japon] ; Tsutomu Ogata [Japon]A 3‐bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia
003469 (2001) Catherine A. Boucher ; Carole A. Sargent ; Tsutomu Ogata ; Nabeel A. AffaraBreakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location [Original article] [Original article]
004526 (1996) Tomonobu Hasegawa [Japon] ; Tsutomu Ogata [Japon] ; Yukihiro Hasegawa [Japon] ; Masataka Honda [Japon] ; Toshiro Nagai [Japon] ; Yoshimitsu Fukushima [Japon] ; Yutaka Nakahori [Japon] ; Nobutake Matsuo [Japon]Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: A clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata
004F43 (1995) Tsutomu Ogata [Japon] ; Nobutake Matsuo [Japon]Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features
007680 (2010) Harunosuke Kato [Japon] ; Rie Yoshida [Japon] ; Katsuhiko Tsukamoto [Japon] ; Hirotaka Suga [Japon] ; Hitomi Eto [Japon] ; Takuya Higashino [Japon] ; Jun Araki [Japon] ; Tsutomu Ogata [Japon] ; Kotaro Yoshimura [Japon]Familial cases of atypical clinical features genetically diagnosed as LEOPARD syndrome (multiple lentigines syndrome)

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